mutations

Englisch - Türkisch

Definition von mutations im Englisch Türkisch wörterbuch

{i} mutasyon

Bu hastalık nadir bir genetik mutasyon tarafından oluşur. - This disease is caused by a rare genetic mutation.

Mutasyonların kökeni kirletilmiş su tüketiminde gibi görünüyor. - It seems that the origin of the mutations is in the consumption of contaminated water.

gene mutations

(Tıp) gen mutasyonları

(Tıp) Ses değişmesi, mütasyon

(Nükleer Bilimler) mutasyon,kalıtsal değişim

mutation

{i} biyol. değişinim, değşinim, mutasyon

mutation

(Sosyoloji, Toplumbilim) değşinim

mutation

{i} değişim

mutation

bir ünlü veya ünsüzün değişmesi

mutation

genleri değişmiş hayvan veya bitki

mutation

{i} dönüşüm

Englisch - Englisch

Definition von mutations im Englisch Englisch wörterbuch: are the changes of a gene from one allelic form to another (i e , the nucleotide sequence changes); plural of mutation; Permanent changes in the genetic material (DNA); changes in the DNA that codes for a gene, which may or may not cause a normal working gene to become a non-working gene; rare changes in the DNA of genes which eventually lead to genetic diversity
frameshift mutations: plural form of frameshift mutation
missense mutations: plural form of missense mutation
mutation: Any heritable change of the base-pair sequence of genetic material
mutation: a mutant
mutation: any alteration or change
nasal mutations: plural form of nasal mutation
nonsense mutations: plural form of nonsense mutation
point mutations: plural form of point mutation
soft mutations: plural form of soft mutation
mutation: the act or process of change
mutation: A change in a gene that can occur randomly (naturally) or that can be deliberately caused in the laboratory by scientists
mutation: a change or alteration in form or qualities
mutation: (genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism
mutation: Gradual definitely tending variation, such as may be observed in a group of organisms in the fossils of successive geological levels
mutation: Change; alteration, either in form or qualities
mutation: A permanent structural alteration in DNA that can be transmitted from one generation to the next Changes in DNA either have no effect or cause harm Occassionally a mutation can improve an organism's chance of surviving and passing the beneficial change on to its descendants
mutation: Change in the structure of a gene or chromosome
mutation: Change of the hereditary information resulting in a change in the sequence of the nucleotides in the DNA
mutation: A term introduced in the late-nineteenth century to refer to large scale phenotypic change but which was appropriated by modern genetics to mean any genetic change, large or small A 'point mutation' is the single substitution of one base A 'translocation' is the reshuffling of a long sequence An 'inversion' is the inverting of a long sequence, and so on
mutation: an alteration or change
mutation: Any inheritable change in DNA sequence
mutation: Any heritable change in the base-pair sequence of genetic material, namely DNA (or RNA in the case of some viruses)
mutation: A permanent structural alteration in DNA In most cases, DNA changes either have no effect or cause harm, but occasionally a mutation can improve an organism's chance of surviving and passing the beneficial change on to its descendants 1
mutation: The occurrence of mutations, and the hereditary transmission, under some conditions, of the characters so appearing, are well-established facts; whether the process has played an important part in the evolution of the existing species and other groups of organisms is a disputed question
mutation: Alteration in the genetic material of a cell that is transmitted to the cell's offspring. Mutations may be spontaneous or induced by outside factors (mutagens). They take place in the genes, occurring when one base is substituted for another in the sequence of bases that determines the genetic code, or when one or more bases are inserted or deleted from a gene. Many mutations are harmless, often masked by the presence of a dominant normal gene (see dominance). Some have serious consequences; for example, a particular mutation inherited from both parents results in sickle-cell anemia. Only mutations that occur in the sex cells (eggs or sperm) can be transmitted to the individual's offspring. Alterations caused by these mutations are usually harmful. In the rare instances in which a mutation produces a beneficial change, the percentage of organisms with this gene will tend to increase until the mutated gene becomes the norm in the population. In this way, beneficial mutations serve as the raw material of evolution
mutation: n (myoo-TAY-shun) Change in a gene or chromosome resulting in a new trait or characteristic that can be inherited Mutation can be a source of beneficial genetic variation, or it can be neutral or harmful in effect
mutation: Any nucleotide change in DNA sequence
mutation: An error in replication or other alteration of the nucleotide base sequence creating a change in the sequence of base pairs on a DNA molecule If the change occurs in the DNA of a somatic cell, the mutation may cause a change in the organism's phenotype (leading, for example, to cancer) but will not affect the organism's offspring; only mutations in the germ cells can cause heritable changes in the offspring
mutation: a change in the genetic material within a living cell
mutation: A heritable change in DNA sequence at the level of the gene, the chromosome, or the genome
mutation: A truncation or change in the normal order of molecules in DNA that defines a specific gene A disease-causing mutation in a gene alters the gene blueprint and thus ultimately disrupts the construction of the normal protein encoded by the gene
mutation: a change in the number, arrangement, or molecular sequence of a gene
mutation: {i} act of mutating; change, alteration; state of having inheritable traits that differ from those of the parent; umlaut (Phonetics)
mutation: Any heritable change in DNA sequence See also: polymorphism Return to Top
mutation: A genetic term A mutation is a change in the genetic code from what is considered normal Mutations can occur normally and not all mutations are harmful
mutation: The result of the above process; a suddenly produced variation
mutation: A change in the genetic information
mutation: a change or alteration in form or qualities (genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism
mutation: - A sudden change in the string of DNA that makes up a gene in an organism
mutation: As now employed (first by de Vries), a sudden variation (the offspring differing from its parents in some well-marked character or characters) as distinguished from a gradual variation in which the new characters become fully developed only in the course of many generations
mutation: (biology) an organism that has characteristics resulting from chromosomal alteration
mutation: This term usually refers to a change in the sequence of the gene which codes for a protein If the sequence of the DNA gene is changed in any way, it will usually cause a change in the sequence in amino acids making up the protein that the gene codes for This can be a problem if the mutation is not intentional because it essentially means you are working with the wrong protein However, sometimes we make a mutation in a gene on purpose, such as the one we made to add on the histidines on the end of CFTR We did this by changing (mutating) the sequence of the CFTR gene carried by the baculovirus
mutation: a change in the character of a gene that is perpetuated when a cell divides or a virus replicates
mutation: Any heritable change in genetic material This may be a chemical transformation of an individual gene (a gene or point mutation), which alters its function On the other hand, this change may involve a rearrangement, or a gain or loss of part of a chromosome, which may be microscopically visible This is designated a chromosomal mutation Most mutations are harmful
mutation: a change in a gene
mutation: A mutation is a change in the parent DNA sequence or genetic code caused by exposure to chemicals and radiation
mutation: A change (in the number, arrangement, or molecular sequence ) in the sequence of DNA coding in a gene that occurs by chance, or due to some external influence A permanent, heritable change in a gene or chromosome structure
mutation: A change in the genetic material of a cell